Canonical Allele Identifier: CA1397810679

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119472G= , CM000665.2:g.122119472G=	GRCh38
NC_000003.11:g.121838319G= , CM000665.1:g.121838319G=	GRCh37
NC_000003.10:g.123321009G=	NCBI36
NG_029928.1:g.69111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.928G= MANE Select	ENSP00000332049.2:p.Ala310=
ENST00000264468.9:c.766G=	ENSP00000264468.6:p.Ala256=
ENST00000330540.6:c.928G=	ENSP00000332049.2:p.Ala310=
ENST00000393627.6:c.910G=	ENSP00000377248.2:p.Ala304=
ENST00000469710.5:c.682G=	ENSP00000418988.1:p.Ala228=
ENST00000478741.1:c.770G=
ENST00000493101.5:c.592G=	ENSP00000420230.1:p.Ala198=
NM_001206924.1:c.592G=	NP_001193853.1:p.Ala198=
NM_001206925.1:c.682G=	NP_001193854.1:p.Ala228=
NM_006889.4:c.910G=	NP_008820.3:p.Ala304=
NM_175862.4:c.928G=	NP_787058.4:p.Ala310=
NM_176892.1:c.766G=	NP_795711.1:p.Ala256=
NM_175862.5:c.928G= MANE Select	NP_787058.5:p.Ala310=
NM_001206924.2:c.592G=	NP_001193853.2:p.Ala198=
NM_001206925.2:c.682G=	NP_001193854.2:p.Ala228=
NM_006889.5:c.910G=	NP_008820.4:p.Ala304=
NM_176892.2:c.766G=	NP_795711.2:p.Ala256=